Circulating microvesicle number, function and small RNA content vary with age, gender, smoking status, lipid and hormone profiles

• Published in: Thrombosis research Vol. 156; pp. 65 - 72
• Main Authors: Enjeti, Anoop K, Ariyarajah, Anita, D'Crus, Angel, Seldon, Michael, Lincz, Lisa F
• Format: Journal Article
• Language: English
• Published: United States Elsevier Ltd 01.08.2017
• Subjects: Adult; Age; Age Factors; Cell-Derived Microparticles - metabolism; Female; Flow Cytometry; Gender; Gender Identity; Hematology, Oncology and Palliative Medicine; Humans; Lipids; Male; microRNA; MicroRNAs - genetics; MicroRNAs - metabolism; Microvesicles; Middle Aged; Smoking; Flow cytometry; microRNA; Microvesicles; Gender; Age; Smoking
• ISSN: 0049-3848; 1879-2472
• DOI: 10.1016/j.thromres.2017.04.019

Abstract Background Characterization of circulating microvesicles (MV) in healthy subjects in relation to various biological factors is not well studied. Objectives We evaluated the influence of age, gender, smoking status, lipid and hormone profiles on circulating MV in healthy subjects. Methods Platelet free plasma from 143 volunteer blood donors (males = 80, females = 63) was evaluated by standardized flow cytometry for MV expressing CD41 (platelet-derived), CD105 (endothelial-derived), CD235 (red cell-derived), TF (tissue factor) and phosphatidylserine (PS) MV. Procoagulant function was measured by the Xa based assay (XaCT) and endogenous thrombin potential (ETP) using thrombin generation assay. Results Those ≤ 29 years and ≥ 60 years had higher levels of MV subsets (CD41, CD235, TF and PS) compared to those aged 30–59 years. The median CD41, CD105, CD235, TF and PS expressing MV by flow cytometry were similar or lower in females, whilst procoagulant activity by the XaCT assay was higher (p = 0.002). In smokers (n = 21), certain MV subsets (CD41, TF and PS) and functional activity (ETP) was lower (p < 0.05). Regression analysis showed that MV parameters of CD41, CD105, TF and ETP could be predicted independently by age, whilst smoking predicted for CD105, CD235, TF, PS and ETP. Certain MV parameters also correlated with BMI, lipid and hormone levels. The small RNA and miRNA levels did not differ by age group, smoking status or gender. Conclusions It is important to recognize that differences may arise depending on age, gender, BMI, lipid, hormone levels and smoking status in apparently healthy subjects when evaluating MV for pathogenic potential.